氧化锌对高胶凝性水泥熟料矿物形成及强度的影响

采用工业原料配料，对以硅酸三钙（C3S，C=CaO，S=SiO2）、硫铝酸钙（C4A3 S^-，C=CaO，A=Al2O3，S^-=SO4^2-）为主导矿物的含C4A3 S^-矿物硅酸盐水泥熟料的矿物形成及其强度进行了研究。借助X射线衍射和热重一差热分析研究了矿物形成过程；探讨了微量元素ZnO对熟料性能的影响及在熟料体系中的固溶情况。研究结果表明：生料中掺入ZnO可使C4A3 S^-和CaS等矿物通过低温反应形成，共存于同一熟料体系中，并可提高熟料的强度；过高的ZnO含量亦会降低C4A3 S^-矿物的分解温度。     

混合材对水泥与减水剂适应性的影响研究

通过对掺高效减水剂水泥净浆流动性及流动性损失的测定试验，研究了3种混合材(粉煤灰、水淬高炉矿渣和沸石)在不同替代率情况下对减水剂作用效果的影响。结果表明：水淬高炉矿渣有利于改善减水剂与水泥的适应性，而掺粉煤灰和沸石(尤其是沸石)则会导致减水剂塑化作用的降低，而且浆体流动性损失也有增大趋势。     

Effect of MgO on the composition and properties of alite-sulphoaluminate cement

The effect of MgO on the composition and properties of alite-sulphoaluminate cement clinker with commercial-grade raw materials such as limestone, clay, gypsum and fly ash as starting materials has been investigated in order to confirm results previously obtained with pure raw materials. The experiment results confirm that the addition of MgO at about 2-5% can improve the burnability of raw meal, promote the absorption of free lime and the formation of C₃S and C₄A₃S¯. In addition, it is shown that this can also increase the strength development of the cement and shorten the setting time. When the content of MgO reaches about 8%, the strength of the cement decreases slightly and the setting time is extended.     

机械激活矿渣水泥

用于式高能振动磨机械激活矿渣（炉渣和／或硅灰）水泥。研究表明：经机械激活后．矿渣水泥的颗粒粒度降低，颗粒的比表面积增大。在掺合了矿渣的水泥中硅微粒聚团经机械激活后可有效地分散并作用于水泥中．使矿渣水泥的水化反应括性增强，促进水泥水化反应，降低水泥制品的孔隙度．从而可以提高水泥制品的力学性能。通过Fourier变换红外光谱和核磁共振等方法分析了机械激活作用的机理。     

改善普通水泥耐久性的研究

研究了活性组分及少量的引气剂对水泥性能的影响。实验表明：活性组分或与少量的引气剂复合使用，降低了水泥砂浆的大孔体积和干缩率，提高了其抗渗性、抗化学侵蚀性、抗钢筋锈蚀性，并改善了水泥砂浆的某些力学性能。     

水泥酸溶性的理论计算与试验研究

根据化学反应方程式计算出溶解一定质量的水泥熟料需要盐酸的摩尔数,结果发现该值明显低于测定水泥酸不溶物常用的摩尔数。根据计算结果,通过正交试验获取较佳的条件组合,提出了测定水泥活性组分的酸溶解测定方法。试验表明,测定方案可行,酸不溶物的测定结果与实际混合材掺量的偏差<0.6%。     

T.C.Powcrs模型若干问题的研究

从T.C.Powers水泥石模型出发,提出了描述水泥混凝土材料初始结构的主要参数是初始孔隙率。由此池绎了水泥浆体组成与结构的定量关系,比原模型有更明了的物理意义,研究结果表明,Powers模型在高孔隙率范围内具有适用性,但不适用于低孔隙率硬化水泥浆体,且在低孔隙率条件下不存在28％的固有凝胶孔隙率,水化产物成份和性质是渐变的。     

The role of calcium ions and lignosulphonate plasticiser in the hydration of cement

Experiments involving equilibrium dialysis, conductivity, X-ray diffraction analysis (XRD), differential thermal analysis (DTA) and isothermal titration calorimetry (ITC) have been carried out to investigate the role of calcium ions and polymeric plasticisers in cement/admixture hydration. Results from a study of lignosulphonic acid, sodium salt, acetate as a plasticiser shows that a plasticiser has dual role; one mainly as a kinetic inhibitor (poison) in cement hydration mechanism and the other as a dispersant. Evidence of a weak Ca²⁺ binding to lignosulphonate sulphonic moieties was found at low ionic strengths of 0.1 M using ITC. No evidence of formal Ca²⁺ binding to lignosulphonate sulphonic acid moieties was found using equilibrium dialysis at higher ionic strength of 1 M (ionic strengths of 0.4 M are typically found in Portland cement pore solution), as is often suggested in cement/admixture literature.     

Study of alinite cement hydration by impedance spectroscopy

Two types of alinite cements, Mg-alinite and Zn-alinite, were synthesized using the reagent grade chemicals. Their hydration behavior was compared with ordinary Portland cement (OPC) using impedance spectroscopy (IS) and ²⁹Si nuclear magnetic resonance (NMR) spectroscopy. The bulk resistance in the IS spectra and the intensity ratio of the hydrous (Q₁ and Q₂) to anhydrous (Q₀) phases in the NMR spectra were estimated as the extent of hydration. The results obtained from both techniques were consistent each other. Mg-alinite had a comparable hydration rate to OPC and Zn-alinite exhibited faster hydration kinetics than Mg-alinite.